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Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Global Trade Compliance Trade Controls Senior Manager

Logistics & TransportationPosted on Nov 12
Full-timeLondon, UKNo salary listed

About the Job

Requirements

  • A BA or BS degree is required.
  • Extensive experience in international trade is required.
  • A Licensed Customs Broker credential or equivalent certification is required.
  • Strong familiarity with export-control requirements is required.
  • Strong familiarity with customs-valuation requirements is required.
  • Experience in the pharmaceutical, life-sciences, or another similarly specialized industry is required, along with knowledge of standard export-import processes.
  • Experience strategically managing customs brokers, managed service providers, and consultants with proven results is required.
  • Some knowledge of logistics systems, including Global Trade Management systems, Transportation Management Systems, ERP, and logistics-provider integrations, is required.
  • Strong digital analytical skills using Excel, SharePoint, Alteryx, and other report-writing and analytical tools are required.
  • The ability to conduct trade-compliance training and make complex requirements relatable to different audiences and business processes is required.
  • The ability to drive continuous improvement and transformative change is required.

Responsibilities

  • Provide primary technical review of Global Trade Compliance standard operating procedures for complex customs requirements, including valuation, product classification, country of origin, and export controls.
  • Develop and manage the customs-valuation program, including the commercial customs-valuation standard operating procedure for manufacturing and finished goods, with reconciliation reporting in the United States, Canada, Australia, the United Kingdom, and other countries as required.
  • Manage the clinical-trial-material customs-valuation standard operating procedure for investigational medicine products supplied to clinical markets, and lead in defending this policy with customs authorities as needed.
  • Develop and manage a customs-valuation standard operating procedure for pipeline products, including cell and gene therapies and small molecules, working with Corporate Tax, Supply Chain, and Regulatory to develop financial supply chains that optimize tax and duty positions.
  • Develop and manage a customs-valuation standard operating procedure for purchased material, including a three-way match among purchase orders, commercial invoices, and payments, and report discrepancies as required.
  • Develop and manage a customs-valuation standard operating procedure for material not subject to transaction value, including development material from contract manufacturing organizations, research material from contract research organizations or between Vertex sites, and samples.
  • Develop and manage the export-control program, identifying material and equipment subject to export commodity control classification requirements through automated surveys, data analytics, and company outreach.
  • Establish physical export controls for non-EAR99 material and equipment, leveraging the managed service provider and Global Trade Management export-document systems to ensure required licenses are in place before shipment.
  • Establish technology-control and deemed-export access-control plans for non-EAR99 material and equipment when Vertex controls or owns technology requiring such controls.
  • Refine and manage enterprise restricted-party screening using Oracle Global Trade Management, operated by a managed service provider, covering customers, suppliers, contract manufacturing organizations, contract research organizations, other partners, employees, contractors, and countries or territories subject to trade sanctions.
  • Collaborate with third-party logistics providers and distributors to evaluate and assess screening activities and establish joint escalation processes.
  • Work with Sourcing and Legal to develop export-control contractual language and establish an Incoterms guideline.
  • Oversee the managed service provider’s product classification work for Harmonized Tariff System, Export Commodity Control, and Partner Government Agency coding; own the Product Classification standard operating procedure and act as the internal subject-matter expert on complex issues.
  • Own the Country of Origin standard operating procedure and oversee the managed service provider’s country-of-origin support as needed.
  • Develop and manage anti-boycott reporting processes.
  • Co-manage external trade managed-service partners and consultants, particularly for export control, trade sanctions, and customs valuation.
  • Support the design, implementation, and operation of the Global Trade Management system, integrating master data and operational orders and shipments with internal stakeholders and systems, trade managed-service providers, customs brokers, forwarders, carriers, and third-party logistics providers.
  • Build and maintain technical compliance processes and governance supporting trade operations managers, and help resolve detailed operational questions.
  • Provide leadership in resolving complex customs and export-control requirements to ensure compliant and predictable access for patients and business partners.
  • Help design technical trade guidance and solutions with the Senior Director of Global Trade Compliance to address business needs, regulatory changes, and market access for pipeline products.
  • Support the continued growth and development of the Global Trade Compliance program and build partnerships with stakeholders across Supply Chain, Manufacturing, Commercial, Finance/Tax, Legal, Regulatory R&D, and other functions.
  • Work with regional Global Trade Compliance operations Senior Managers to support the ongoing movement of material.

About the Company

Vertex Pharmaceuticals

Develops therapies for serious genetic diseases

Vertex Pharmaceuticals develops medicines for serious diseases, with a focus on cystic fibrosis. It conducts extensive research and partners with other biotech firms to discover and develop new therapies, including ex vivo engineered cell treatments. Its products, such as ivacaftor, treat cystic fibrosis and other therapies undergo clinical testing to expand the pipeline. Revenue comes from selling approved drugs and from licensing and collaboration agreements. The company distinguishes itself through deep R&D investment, strategic partnerships, and a global reach aimed at addressing unmet medical needs. The overall goal is to bring effective new drugs to patients worldwide and improve outcomes and quality of life.

Company size
5,001-10,000
Company stage
IPO
Headquarters
Boston, MA
Founded
1989

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